HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23387Generated: October 26, 2026
Dimethyl Sulfide → 2-Chloro-6-methylsulfanylmethyl-phenylamine
https://huagongshe.com/reaction/23387
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | 2-Chloroaniline | HCID 7240 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Chloro-6-methylsulfanylmethyl-phenylamine | HCID 326709 | 82% |
Reaction Steps
2-Chloro-phenylamine (12.76 g, 0.1 mole) and dimethyl sulfide (10 ml) were dissolved in dichloroethane (200 ml) and cooled in an ice-acetone-salt bath under a nitrogen atmosphere. N-chlorosuccinimide (14.70 g, 0.11 mole) dissolved in dichloroethane (300 ml) was slowly added via addition funnel over about 20-30 minutes. After stirring an hour beyond addition while allowing the reaction to reach room temperature, triethyl amine (30 ml) was added and the mixture was brought to reflux for 1 h and 20 minutes. The reaction was monitored by tlc (15:85 EtOAc:hexane on silica gel) which showed a single less polar product. The mixture was cooled and evaporated to dryness. The residue was taken up in methylene chloride, dry packed on silica gel, and placed onto a column of flash silica gel. The product was eluted from the column with 1:9 ethyl acetate:hexane to give 15.4 g of a homogeneous oil (82%), 2-chloro-6-methylsulfanylmethyl-phenylamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06852726B2 |
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| Source dataset | uspto-grants-2005_02 |
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| ORD ID | ord-33e3ac922d8e4f8d978a1b211f1d4a44 |
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| Source note | uspto-grants-2005_02 |
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